Abstract
Abstract In-situ two-dimensional X-ray absorption spectroscopy (XAS) imaging was employed to analyze cerium ion (Ce3+) migration in the through-plane direction in proton exchange membrane fuel cells (PEMFCs), offering fundamental insights supporting improvement of their power density and membrane durability. The transport of Ce3+ was visualized in both unreinforced thick Nafion membranes (Nafion 115, 127 µm) and reinforced thin (12 µm) perfluorosulfonic acid (PFSA) membranes under either an electrical potential gradient or a water activity gradient. The diffusion coefficients of Ce3+ were ascertained based on its behavior after removal of these gradients in both membrane types. Additionally, using a one-dimensional cation transport model, the mobility and electroosmotic drag coefficients of Ce3+ were derived from experimentally obtained data of the thick Nafion membrane. Our measurements also demonstrate that the migration of Ce3+ in the thick membranes was notably impeded by the presence of ferrous ion (Fe2+) impurities. Because Fe2+ is known to accelerate membrane degradation by promoting hydroxyl radical formation, this effect might further exacerbate membrane degradation. It therefore warrants careful consideration.
Published Version
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